Mara Doimo

1.8k total citations
25 papers, 944 citations indexed

About

Mara Doimo is a scholar working on Molecular Biology, Electrical and Electronic Engineering and Biochemistry. According to data from OpenAlex, Mara Doimo has authored 25 papers receiving a total of 944 indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 9 papers in Electrical and Electronic Engineering and 8 papers in Biochemistry. Recurrent topics in Mara Doimo's work include Coenzyme Q10 studies and effects (11 papers), Mitochondrial Function and Pathology (9 papers) and Advanced battery technologies research (9 papers). Mara Doimo is often cited by papers focused on Coenzyme Q10 studies and effects (11 papers), Mitochondrial Function and Pathology (9 papers) and Advanced battery technologies research (9 papers). Mara Doimo collaborates with scholars based in Italy, Spain and Sweden. Mara Doimo's co-authors include Leonardo Salviati, Eva Trevisson, María Andrea Desbats, Plácido Navas, Matteo Cassina, Cristina Cerqua, Alberto Casarin, Carlos Santos‐Ocaña, Sjoerd Wanrooij and Giuseppe Basso and has published in prestigious journals such as Journal of the American Chemical Society, Nucleic Acids Research and Journal of Biological Chemistry.

In The Last Decade

Mara Doimo

25 papers receiving 935 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Mara Doimo Italy 19 846 274 269 120 42 25 944
Vanna Géromel France 10 708 0.8× 162 0.6× 153 0.6× 133 1.1× 34 0.8× 13 811
Antonio Arroyo Spain 8 326 0.4× 65 0.2× 59 0.2× 13 0.1× 26 0.6× 9 521
Lili Xia China 15 421 0.5× 32 0.1× 169 0.6× 8 0.1× 20 0.5× 30 776
Justina Šileikytė Italy 14 695 0.8× 47 0.2× 15 0.1× 89 0.7× 31 0.7× 19 853
Elena S. Dremina United States 13 371 0.4× 22 0.1× 43 0.2× 20 0.2× 14 0.3× 18 531
Viktoria Kheifets United States 10 552 0.7× 11 0.0× 49 0.2× 180 1.5× 15 0.4× 12 646
Tadashi Aogaichi United States 12 304 0.4× 27 0.1× 62 0.2× 97 0.8× 13 0.3× 15 463
Gerhard Plaut United States 14 302 0.4× 24 0.1× 71 0.3× 94 0.8× 8 0.2× 25 492
Weina Han China 12 273 0.3× 44 0.2× 56 0.2× 7 0.1× 15 0.4× 33 582
P Nagley Australia 12 643 0.8× 22 0.1× 24 0.1× 108 0.9× 10 0.2× 17 739

Countries citing papers authored by Mara Doimo

Since Specialization
Citations

This map shows the geographic impact of Mara Doimo's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Mara Doimo with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Mara Doimo more than expected).

Fields of papers citing papers by Mara Doimo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mara Doimo. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Mara Doimo. The network helps show where Mara Doimo may publish in the future.

Co-authorship network of co-authors of Mara Doimo

This figure shows the co-authorship network connecting the top 25 collaborators of Mara Doimo. A scholar is included among the top collaborators of Mara Doimo based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Mara Doimo. Mara Doimo is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Nguyen, Tran, Farahnaz Ranjbarian, I.C. Mendes, et al.. (2025). Activating AMPK improves pathological phenotypes due to mtDNA depletion. FEBS Journal. 292(9). 2359–2380. 2 indexed citations
2.
Doimo, Mara, Namrata Chaudhari, Tran Nguyen, et al.. (2023). Enhanced mitochondrial G-quadruplex formation impedes replication fork progression leading to mtDNA loss in human cells. Nucleic Acids Research. 51(14). 7392–7408. 29 indexed citations
3.
Prasad, Bagineni, et al.. (2022). A complementary chemical probe approach towards customized studies of G-quadruplex DNA structures in live cells. Chemical Science. 13(8). 2347–2354. 22 indexed citations
4.
Kasho, Kazutoshi, Gorazd Stojkovič, María I. Martínez-Jiménez, et al.. (2021). A unique arginine cluster in PolDIP2 enhances nucleotide binding and DNA synthesis by PrimPol. Nucleic Acids Research. 49(4). 2179–2191. 10 indexed citations
5.
Uhler, Jay P., Anna‐Karin Berglund, Bradley Peter, et al.. (2018). A two-nuclease pathway involving RNase H1 is required for primer removal at human mitochondrial OriL. Nucleic Acids Research. 46(18). 9471–9483. 24 indexed citations
6.
Cerqua, Cristina, Valeria Morbidoni, María Andrea Desbats, et al.. (2018). COX16 is required for assembly of cytochrome c oxidase in human cells and is involved in copper delivery to COX2. Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1859(4). 244–252. 25 indexed citations
7.
Montioli, Riccardo, María Andrea Desbats, Silvia Grottelli, et al.. (2018). Molecular and cellular basis of ornithine δ-aminotransferase deficiency caused by the V332M mutation associated with gyrate atrophy of the choroid and retina. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1864(11). 3629–3638. 13 indexed citations
8.
Vázquez-Fonseca, Luis, Mara Doimo, María Andrea Desbats, et al.. (2017). Mutations in COQ8B (ADCK4) found in patients with steroid-resistant nephrotic syndrome alter COQ8B function. Human Mutation. 39(3). 406–414. 36 indexed citations
9.
Desbats, María Andrea, Valeria Morbidoni, Micol Silic‐Benussi, et al.. (2016). TheCOQ2genotype predicts the severity of coenzyme Q10deficiency. Human Molecular Genetics. 25(19). 4256–4265. 45 indexed citations
10.
Desbats, María Andrea, Annalisa Vetro, Ivan Limongelli, et al.. (2015). Primary coenzyme Q10 deficiency presenting as fatal neonatal multiorgan failure. European Journal of Human Genetics. 23(9). 1254–1258. 39 indexed citations
11.
Doimo, Mara, Raffaele Lopreiato, Alessandra Tessa, et al.. (2015). Heterologous Expression in Yeast of Human Ornithine Carriers ORNT1 and ORNT2 and of ORNT1 Alleles Implicated in HHH Syndrome in Humans. JIMD Reports. 28. 119–126. 4 indexed citations
12.
Nguyen, Theresa, Alberto Casarin, María Andrea Desbats, et al.. (2014). Molecular characterization of the human COQ5 C-methyltransferase in coenzyme Q10 biosynthesis. Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids. 1841(11). 1628–1638. 47 indexed citations
13.
Doimo, Mara, María Andrea Desbats, Cristina Cerqua, et al.. (2014). Genetics of Coenzyme Q10 Deficiency. Molecular Syndromology. 5(3-4). 156–162. 94 indexed citations
14.
Doimo, Mara, Eva Trevisson, Rannar Airik, et al.. (2013). Effect of vanillic acid on COQ6 mutants identified in patients with coenzyme Q10 deficiency. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1842(1). 1–6. 67 indexed citations
15.
Salviati, Leonardo, Eva Trevisson, María Hernández, et al.. (2012). Haploinsufficiency of COQ4 causes coenzyme Q10 deficiency. Journal of Medical Genetics. 49(3). 187–191. 85 indexed citations
16.
Casarin, Alberto, Vanessa Pertegato, Roberta Siviero, et al.. (2012). Copper and bezafibrate cooperate to rescue cytochrome c oxidase deficiency in cells of patients with sco2 mutations. Orphanet Journal of Rare Diseases. 7(1). 21–21. 26 indexed citations
17.
Casarin, Alberto, Mara Doimo, Eva Trevisson, et al.. (2009). X‐linked brachytelephalangic chondrodysplasia punctata: A simple trait that is not so simple. American Journal of Medical Genetics Part A. 149A(11). 2464–2468. 9 indexed citations
18.
Trevisson, Eva, Alberto Burlina, Mara Doimo, et al.. (2009). Functional Complementation in Yeast Allows Molecular Characterization of Missense Argininosuccinate Lyase Mutations. Journal of Biological Chemistry. 284(42). 28926–28934. 27 indexed citations
19.
Casarin, Alberto, Eva Trevisson, Vanessa Pertegato, et al.. (2008). Functional characterization of human COQ4, a gene required for Coenzyme Q10 biosynthesis. Biochemical and Biophysical Research Communications. 372(1). 35–39. 43 indexed citations
20.
Salviati, Leonardo, Eva Trevisson, Mara Doimo, & Plácido Navas. (1993). Primary Coenzyme Q 10 Deficiency. 22 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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